FIDIA FARMACEUTICI S.P.A

FDA Device Registration & Listing · Paderno Dugnano Milano, IT · Registration 3017870985

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017870985
FEI Number
3017870985
Entity Name
FIDIA FARMACEUTICI S.P.A
City/State/Country
Paderno Dugnano Milano, IT
Establishment Address
Via Ampere 19/21, Paderno Dugnano Milano 20037, IT
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Fidia Farmaceutici S.P.A (Owner Number: 10079382)
Owner / Operator Contact Address
Via Ampere 19/21, Paderno Dugnano, IT-MI 20037, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Gasa Esteril/Sterile Gauze

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2020-12-03

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Fidia Farmaceutici S.P.A
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3013391391 HERKIMER COUNTY CHAPTER NYSARC, INC. Herkimer, NY, US
3012677665 TECHNO PLASTICS INDUSTRIES, INC. Anasco, PR, US
3038131023 UNITED TECHNOLOGY VIETNAM COMPANY LIMITED Quang Ha Commune Quang Ninh, VN
3005360866 QEL DOMINICANA S.A. ESPERANZA Valverde, DO
3043106338 SHENZHEN SPONGE NEW MATERIAL CO. LTD Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017870985. Last updated year: 2026. Please use registration number 3017870985 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.